Canonical Allele Identifier: CA472436486
Gene: DRD4 HGNC NCBI

Linked Data

dbSNP Id: rs1370671469
gnomAD v2: 11-637589-G-A
gnomAD v4: 11-637589-G-A
MyVariant Identifiers: chr11:g.637589G>A (hg19) chr11:g.637589G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.637589G>A , CM000673.2:g.637589G>A GRCh38
NC_000011.9:g.637589G>A , CM000673.1:g.637589G>A GRCh37
NC_000011.8:g.627589G>A NCBI36
NG_021241.1:g.5285G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000176183.6:c.285G>A MANE Select ENSP00000176183.5:p.Glu95=
ENST00000176183.5:c.285G>A ENSP00000176183.5:p.Glu95=
NM_000797.3:c.285G>A NP_000788.2:p.Glu95=
NM_000797.4:c.285G>A MANE Select NP_000788.2:p.Glu95=
Search 100 bp 5'
Search 100 bp 3'